510(k) K102606 ยท OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
AVS ANCHOR-C CERVICAL CAGE SYSTEM
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Apr 22, 2011 |
| Received | Sep 10, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102606
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 23, 2024 | Stryker Spine AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at Open, Classified |
OVE | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.